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Progenetix - genomic copy number aberrations in cancer
The Progenetix database provides an overview of copy number abnormalities in human cancer from Comparative Genomic Hybridization (CGH) experiments. With 30817 cases from 1016 publications (Oct 2013), Progenetix is the largest curated database for who
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Condel
Method to assess the outcome of non-synonymous SNVs using a CONsensus DELeteriousness score that combines various tools.
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The mitochondrial DNA breakpoints database
A comprehensive on-line resource with curated datasets of mitochondrial DNA (mtDNA) rearrangements.
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PanDrugs
PanDrugs is a method to prioritize anticancer drug treatments according to individual genomic data. PanDrugs current version integrates data from 24 primary sources and supports 56297 drug-target associations obtained from 4804 genes and 9092 unique
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MutationAligner
Somatic mutation hotspots in protein domains in cancer
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HDAM
A resource of human disease associated mutations from next generation sequencing studies.
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STRipy
A graphical application for detecting known pathogenic short tandem repeats in sequencing data
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EVmutation
A statistical method for predicting the effects of mutations.
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*ReputationScore indicates how established a given datasource is. Find out more.